Methyl 4-(3-aminophenyl)thiazole-2-carboxylate

≥95%

Reagent Code: #205497
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CAS Number 885279-72-1

science Other reagents with same CAS 885279-72-1

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scatter_plot Molecular Information
Weight 234.28 g/mol
Formula C₁₁H₁₀N₂O₂S
badge Registry Numbers
MDL Number MFCD06738749
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly in the development of kinase inhibitors and anti-inflammatory agents. Its structure supports binding to enzyme active sites, making it valuable in designing drugs for cancer and neurological disorders. Also employed in the preparation of fluorescent probes for cellular imaging due to its favorable photophysical properties. Commonly utilized in medicinal chemistry for scaffold modification to enhance drug potency and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,770.00

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Methyl 4-(3-aminophenyl)thiazole-2-carboxylate
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Used in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly in the development of kinase inhibitors and anti-inflammatory agents. Its structure supports binding to enzyme active sites, making it valuable in designing drugs for cancer and neurological disorders. Also employed in the preparation of fluorescent probes for cellular imaging due to its favorable photophysical properties. Commonly utilized in medicinal chemistry for scaffold modification to enhanc

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly in the development of kinase inhibitors and anti-inflammatory agents. Its structure supports binding to enzyme active sites, making it valuable in designing drugs for cancer and neurological disorders. Also employed in the preparation of fluorescent probes for cellular imaging due to its favorable photophysical properties. Commonly utilized in medicinal chemistry for scaffold modification to enhance drug potency and selectivity.

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